Nuwellis, Inc.
1 recall(s) on record — most severe on record: Class I.
Activity by year
- Recalls (1)
- Inspections (2)
Devices registered here (2)
- Catheter, Hemodialysis, Non-Implanted, Ultrafiltration, For Peripheral UseProduct code NQJ (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5540
- Catheter, Hemodialysis, Non-ImplantedProduct code MPB (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5540
Recalls & enforcement
- Class ICompleted2024-12-11The AquaFlexFlow UF 500 Plus extracorporeal blood circuit used with the Aquadex SmartFlow and FlexFlow Systems may indicate "Ultrafiltrate Weight Mismatch" or Excessive Weight Mismatch Alarms while in use. If not addressed, this failure could result in excess fluid removal from…
FDA inspections (2)
- NAI2023-04-13No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- NAI2016-12-06No Action Indicated · Compliance: Devices
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Nuwellis, Inc. (FEI 3007137787) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007137787-nuwellis-inc/
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